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FDA Inspection
•Hetero Drugs Ltd. - Unit 1•February 25, 2016

Hetero Drugs Ltd. - Unit 1 – FDA Inspection, Feb 25, 2016

Record Details

This FDA Inspection record concerns Hetero Drugs Ltd. - Unit 1, with an inspection on February 25, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Hetero Drugs Ltd. - Unit 1
Inspection Date
February 25, 2016
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · da490c83-d41b-4116-a50a-bf9494179cfa

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
963050
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Hetero Drugs Ltd. - Unit 1

5
DateClassificationOfficeProject area
May 16, 2025Not classifiedOffice of Inspections and Investigations
February 14, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 2, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 2, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 11, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Hetero Drugs Ltd. - Unit 1
  • FDA Inspection 1269555 - 2025-05-16
  • FDA Inspection 1121294 - 2020-02-14
  • FDA Inspection 1044698 - 2018-03-02
  • FDA Inspection 888747 - 2014-05-02
  • FDA Inspection 700761 - 2010-11-11

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